Canonical Allele Identifier: CA2580085168
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1769065
ClinVar RCV Id: RCV002383282

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717967delinsCA , CM000674.2:g.12717967delinsCA GRCh38
NC_000012.11:g.12870901delinsCA , CM000674.1:g.12870901delinsCA GRCh37
NC_000012.10:g.12762168delinsCA NCBI36
NG_016341.1:g.5600delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.128delinsCA ENSP00000507272.1:p.Arg43ProfsTer?
ENST00000682620.1:n.1631-858delinsCA
ENST00000684771.1:n.585-858delinsCA
ENST00000228872.9:c.128delinsCA MANE Select ENSP00000228872.4:p.Arg43ProfsTer?
ENST00000228872.8:c.128delinsCA ENSP00000228872.4:p.Arg43ProfsTer?
ENST00000396340.1:c.128delinsCA ENSP00000379629.1:p.Arg43ProfsTer?
ENST00000442489.1:c.107delinsCA ENSP00000407597.1:p.Arg36ProfsTer?
ENST00000477087.1:n.155-858delinsCA
NM_004064.4:c.128delinsCA NP_004055.1:p.Arg43ProfsTer?
NM_004064.5:c.128delinsCA MANE Select NP_004055.1:p.Arg43ProfsTer?